SCHEMBL182500

SCHEMBL182500

O=C(OC12CC3CC(CC(C3)C1)C2)c1ccc(NCc2cc(O)ccc2O)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
HSP90AA1 P07900 3/20 1.00
CKS1B P61024 2/20 1.00
SKP2 Q13309 2/20 1.00
SKP1 P63208 1/20 1.00
HKDC1 Q2TB90 1/20 0.63
EGFR P00533 12/20 0.58
SYK P43405 2/20 0.49
CA1 P00915 1/20 0.49
CA2 P00918 1/20 0.49
RGS12 O14924 1/20 0.47
ALDH1A1 P00352 1/20 0.47
LCK P06239 1/20 0.47
MAPT P10636 1/20 0.47
CAMKK2 Q96RR4 1/20 0.47
NOX4 Q9NPH5 1/20 0.47
TDP1 Q9NUW8 1/20 0.47

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL29375858 1.00 HSP90AA1 (1.00) HSP90AA1CKS1BSKP2SKP1HKDC1
SCHEMBL14431702 0.87 HSP90AA1 (0.77) HSP90AA1CKS1BSKP2SKP1HKDC1
SCHEMBL415185 0.85 CKS1B (1.00) HSP90AA1CKS1BSKP2SKP1HKDC1
SCHEMBL16279523 0.83 CKS1B (0.81) HSP90AA1CKS1BSKP2SKP1HKDC1
SCHEMBL15536091 0.81 HSP90AA1 (0.68) HSP90AA1CKS1BSKP2SKP1HKDC1
SCHEMBL18263261 0.81 CKS1B (0.67) HSP90AA1CKS1BSKP2SKP1HKDC1
SCHEMBL182501 0.80 HSP90AA1 (0.67) HSP90AA1CKS1BSKP2SKP1HKDC1
SCHEMBL4973506 0.80 HSP90AA1 (0.67) HSP90AA1CKS1BSKP2SKP1HKDC1
Adamantane SCHEMBL27774428 0.80 HSP90AA1 (0.66) HSP90AA1CKS1BSKP2SKP1HKDC1
SCHEMBL5794016 0.78 HKDC1 (1.00) HSP90AA1CKS1BSKP2SKP1HKDC1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 1716 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9976172-B2 Method and apparatus for measuring protein post-translational modification ICAGEN, INC. (US) 2018-05-22 US claimed
CN-101896177-A Combination of therapeutic agents for the treatment of cancer NOVARTIS AG 2010-11-24 CN claimed
US-20100272717-A1 COMBINATIONS OF THERAPEUTIC AGENTS FOR TREATING CANCER NOVARTIS AG (CH) 2010-10-28 US claimed
US-12637415-B2 Lyophilized composition comprising (s)-isopropyl 2-((s)-2-acetamido-3-(1H-indol-3-yl)propanamido)-6-diazo-5-oxohexanoate for intravenous administration and the use thereof DRACEN PHARMACEUTICALS, INC. (US) 2026-05-26 US disclosed
US-12637473-B2 MDM2 protein degraders REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2026-05-26 US disclosed
US-12624044-B2 SMARCA degraders and uses thereof KYMERA THERAPEUTICS, INC. (US) 2026-05-12 US disclosed
US-20260124309-A1 STAT6 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2026-05-07 US disclosed
US-20260125397-A1 MK2 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2026-05-07 US disclosed
US-20260125400-A1 TYK2 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2026-05-07 US disclosed
US-12617777-B2 GPR84 antagonists and uses thereof Liminal Biosciences Limited (GB) 2026-05-05 US disclosed
US-12616679-B2 Lyophilized composition comprising (s)-isopropyl 2-((s)-2-acetamido-3-(1H-indol-3-yl)propanamido)-6-diazo-5-oxohexanoate for subcutaneous administration and the use thereof DRACEN PHARMACEUTICALS, INC. (US) 2026-05-05 US disclosed
US-20050222171-A1 Organic compounds NOVARTIS AG (CH) 2005-10-06 US disclosed
WO-2005070431-A1 PYRAZOLO[1,5-A]PYRIMIDIN-7-YL-AMINE DERIVATIVES FOR USE IN THE TREATMENT OF PROTEIN KINASE DEPENDENT DISEASES NOVARTIS AG (CH) 2005-08-04 WO disclosed
WO-2005053704-A1 METHOD FOR PREDICTING DRUG RESPONSIVENESS IN MYELOID NEOPLASMS NOVARTIS AG (CH) 2005-06-16 WO disclosed
WO-2005054238-A1 1H-IMIDAZO[4,5-C]QUINOLINE DERIVATIVES IN THE TREATMENT OF PROTEIN KINASE DEPENDENT DISEASES NOVARTIS AG (CH) 2005-06-16 WO disclosed
WO-2005054237-A1 1H-IMIDAZOQUINOLINE DERIVATIVES AS PROTEIN KINASE INHIBITORS NOVARTIS AG (CH) 2005-06-16 WO disclosed
US-20050113384-A1 Combinations of (a) an atp-competitive inhibitor of c-acl kinase activity with (b) two or more other antineoplastic agents AVRAMIS IOANNIS A (US) 2005-05-26 US disclosed
WO-2005027972-A2 COMBINATION OF A VEGF RECEPTOR INHIBITOR WITH A CHEMOTHERAPEUTIC AGENT NOVARTIS AG (CH) 2005-03-31 WO disclosed
EP-1441717-A1 COMBINATION OF AN ATP-COMPETITIVE INHIBITOR OF BCR/ABL KINASE ACTIVITY AND A TYRPHOSTIN ANALOG MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2004-08-04 EP disclosed
WO-2003037322-A1 COMBINATION OF AN ATP-COMPETITIVE INHIBITOR OF BCR/ABL KINASE ACTIVITY AND A TYRPHOSTIN ANALOG MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2003-05-08 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (11 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-12637473-B2 MDM2 protein degraders MDM2, TP53, TP53BP1 HSP90AA1 833/4885CKS1B 93/4885SKP2 75/4885
US-20260125400-A1 TYK2 DEGRADERS AND USES THEREOF TYK2, CSNK2A1, CSNK2A2 HSP90AA1 2926/4885CKS1B 425/4885SKP2 676/4885
US-20260124309-A1 STAT6 DEGRADERS AND USES THEREOF STAT6, NCOR2, NCOR1 HSP90AA1 4165/4885CKS1B 1696/4885SKP2 1193/4885
US-20100272717-A1 COMBINATIONS OF THERAPEUTIC AGENTS FOR TREATING CANCER ANXA5, BAX, ANXA6 HSP90AA1 1326/4885CKS1B 2774/4885SKP2 2385/4885
US-12617777-B2 GPR84 antagonists and uses thereof GPR84, GPR88, GPR3 HSP90AA1 3418/4885CKS1B 1690/4885SKP2 1215/4885
US-20050222171-A1 Organic compounds JAK1, MAP3K5, MAP3K7 HSP90AA1 3121/4885CKS1B 424/4885SKP2 267/4885
US-20260125397-A1 MK2 DEGRADERS AND USES THEREOF NR2C2, NR3C2, OXER1 HSP90AA1 2935/4885CKS1B 425/4885SKP2 400/4885
US-12616679-B2 Lyophilized composition comprising (s)-isopropyl 2-((s)-2-acetamido-3-(1H-indol-3-yl)propanamido)-6-diazo-5-oxohexanoate for subcutaneous administration and the use thereof GLUL, QPCT, QPCTL HSP90AA1 4495/4885CKS1B 1625/4885SKP2 1021/4885
US-12624044-B2 SMARCA degraders and uses thereof SMARCA1, SMARCC1, SMARCA2 HSP90AA1 1649/4885CKS1B 145/4885SKP2 485/4885
US-20050113384-A1 Combinations of (a) an atp-competitive inhibitor of c-acl kinase activity with (b) two or more other antineoplastic agents AURKC, CLK1, TTK HSP90AA1 790/4885CKS1B 26/4885SKP2 153/4885
US-12637415-B2 Lyophilized composition comprising (s)-isopropyl 2-((s)-2-acetamido-3-(1H-indol-3-yl)propanamido)-6-diazo-5-oxohexanoate for intravenous administration and the use thereof GLS, GLUL, GLS2 HSP90AA1 3904/4885CKS1B 3310/4885SKP2 1125/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.